Автор: A Messore · 2020 · Цитируется: 16 — pyrrolyl−pyrazoles demonstrated inhibitory activities within the (PDF). □ AUTHOR INFORMATION. Corresponding Author. 15 сент. 2010 г. — Abstract. The preparation of pyrazole derivatives involving a 1,3-dipolar cycloaddition between a diazomethane (or other diazonium salt) and a Автор: RN Butler · 2008 · Цитируется: 120 — It was successful with 1-(p-anisyl)pyrazoles, 2-(p-anisyl)-1,2,3-triazoles, 2-(p-anisyl)-2H-tetrazoles, jo702423z-file003.pdf (7.32 MB)Download PDF. New one-pot synthesis of pyrazole-5-carboxylates by 1,3-dipole cycloadditions of ethyl diazoacetate with [alpha]-methylene carbonyl compounds Автор: G Vinciarelli · 2022 — The reaction is pH dependent, as in the presence of protic catalysis (H 2 SO 4 4%, pH 3.5) a mixture of 3,5- and 4,5-disubstituted pyrazoles was Автор: CB Vicentini · 1990 · Цитируется: 15 — A new general and efficient synthesis of imidazo[4,5-c]pyrazoles (5) is reported. The key step of this synthetic procedure is the intramolecular Автор: P Mellini · 2018 — Correction to 'Pyrazole-based inhibitors of enhancer of zeste homologue 2 induce apoptosis and autophagy in cancer cells'. Solvent-Free 1H-tetrzole, 1,2,5,6-tetrahydronicotinonitrile and pyrazole synthesis using Quinoline Based Ionic Fluoride Salts (QuFs): Thermal and. Full Text PDF Links found: Three-component synthesis of C2F5-substituted pyrazoles from C2F5CH2NH2·HCl, NaNO2 and electron-deficient alkynes. Автор: P Mellini · 2018 — Correction to 'Pyrazole-based inhibitors of enhancer of zeste homologue 2 induce apoptosis and autophagy in cancer cells'. Paolo Mellini.